510(k) K880264 ยท HXY Brace, Drill
BONE SUTURE FIXATION DEVICE
| Applicant | Orthopedic Systems, Inc., Hayward CA, US |
| Decision | Substantially Equivalent for Some Indications, Mar 23, 1988 |
| Received | Jan 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880264
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.